David E Godler
Overview
Explore the profile of David E Godler including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
50
Citations
472
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Godler D, Singh D, Butler M
Curr Opin Psychiatry
. 2025 Jan;
38(2):95-100.
PMID: 39804213
Purpose Of Review: Prader-Willi (PWS) and Angelman (AS) syndromes arise from errors in 15q11-q13 imprinting. This review describes recent advances in genomics and how these expand our understanding of these...
2.
Alshawsh M, Wake M, Gecz J, Corbett M, Saffery R, Pitt J, et al.
Epigenomics
. 2024 Oct;
16(18):1203-1214.
PMID: 39365098
This study describes a protocol to assess a novel workflow called Epi-Genomic Newborn Screening (EpiGNs) on 100,000 infants from the state of Victoria, Australia. The workflow uses a first-tier screening...
3.
Godler D, Inaba Y, Bui M, Francis D, Skinner C, Schwartz C, et al.
Int J Mol Sci
. 2023 Jul;
24(13).
PMID: 37445892
This study characterizes the DNA methylation patterns specific to fragile X syndrome (FXS) with a full mutation (FM > 200 CGGs), premutation (PM 55-199 CGGs), and X inactivation in blood...
4.
Godler D, Brown W
Genes (Basel)
. 2023 Jun;
14(6).
PMID: 37372328
Fragile X syndrome (FXS) is the leading single-gene cause of inherited intellectual disability and autism [...].
5.
Hartmanis S, Baker E, Godler D, Liew D
Disabil Health J
. 2023 Jan;
16(2):101423.
PMID: 36639256
Background: Angelman syndrome (AS) is a rare genetic condition characterized by global developmental delay, including severe intellectual disability. The parents of persons with AS experience increased stress, anxiety, and depression....
6.
Baker E, Arpone M, Bui M, Kraan C, Ling L, Francis D, et al.
Am J Med Genet A
. 2022 Nov;
191(2):357-369.
PMID: 36349505
Fragile X syndrome (FXS) is caused by hypermethylation of the FMR1 promoter due to the full mutation expansion (full mutation [FM]: CGG ≥ 200 repeats) and silencing of FMR1. Assessment...
7.
Crompton K, Godler D, Ling L, Elwood N, Mechinaud-Heloury F, Raj T, et al.
Cells Tissues Organs
. 2022 Oct;
212(6):546-553.
PMID: 36261026
Umbilical cord blood cells have therapeutic potential for neurological disorders, through a paracrine mechanism of action. A greater understanding of the safety and immunological effects of allogeneic donor cord blood...
8.
Arpone M, Bretherton L, Amor D, Hearps S, Rogers C, Field M, et al.
Res Dev Disabil
. 2022 Sep;
131:104338.
PMID: 36179574
Background: Despite the increasing number of clinical trials involving children with neurodevelopmental disorders, appropriate and objective outcome measures for behavioral symptoms are still required. Aim: This study assessed the agreement...
9.
Baker E, Merton C, Tan W, Dudding-Byth T, Godler D, Sadhwani A
Eur J Med Genet
. 2022 Feb;
65(4):104456.
PMID: 35218942
Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by loss of expression of the maternally-inherited UBE3A on chromosome 15q11.2. In AS due to a chromosomal deletion that encompasses UBE3A,...
10.
Godler D, Ling L, Gamage D, Baker E, Bui M, Field M, et al.
JAMA Netw Open
. 2022 Jan;
5(1):e2141911.
PMID: 34982160
Importance: Newborn screening for Angelman syndrome (AS), Prader-Willi syndrome (PWS), and chromosome 15 duplication syndrome (Dup15q) may lead to benefit from early diagnosis and treatment. Objective: To examine the feasibility...